ALKALINE CORP.

FDA Device Registration & Listing · EATONTOWN, NJ, US · Registration 2248704

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
2248704
FEI Number
1000526882
Entity Name
ALKALINE CORP.
City/State/Country
EATONTOWN, NJ, US
Establishment Address
38 Industrial Way E Ste 3A, EATONTOWN, NJ 07724, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
ALKALINE CORP. (Owner Number: 9023828)
Owner / Operator Contact Address
20 MERIDIAN ROAD SUITE 9, --, EATONTOWN, NJ 07724, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K844221
PMA Number
N/A

All Registered Proprietary Names

Morrow Brown Allergy Test Needle

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
SCL Allergen And Vaccine Delivery Needles General Hospital Class 2 880.5570 2008-10-17

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ALKALINE CORP.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K000299 Biomedex, Inc. DERMAPIK II SKIN TEST SYSTEM, DERMAPIK II (SINGLE TEST DEVICE), POLYPIK II (MULTIPLE SKIN TEST DEVICE), DERMAPIK TRAY, D 2000-04-28

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2248704. Last updated year: 2026. Please use registration number 2248704 when referencing this establishment in official correspondence.
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